OBO ID: DOID:0060786 |
Term Name: | hypomyelinating leukodystrophy | Search Ontology: | |
---|---|---|---|
Synonyms: |
|
||
Definition: | A leukodystrophy characterized by improper formation of the myelin sheath in the central nervous system resulting in T2 hyperintensity and variable T1 signal on magnetic resonance imaging. (3) | ||
References: | |||
Ontology: | Human Disease ( DOID:0060786 ) |
OTHER hypomyelinating leukodystrophy PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
Fish | Conditions | Citations |
---|---|---|
AB/TU + MO2-degs1 | standard conditions | Pant et al., 2019 |
ck1Tg + MO2-degs1 | standard conditions | Pant et al., 2019 |
PHENOTYPE
No data available
CITATIONS (2)
Your Input Welcome
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if
additional information is required.
Oops. Something went wrong. Please try again later.